Plasma arginine and citrulline concentrations in critically ill children: strong relation with inflammation

Dick A van Waardenburg1, Carlijn T de Betue, Yvette C Luiking

  • 1Department of Pediatrics, University Hospital Maastricht, Maastricht, Netherlands. dcwa@paed.azm.nl

Insights

Critically ill children with sepsis or trauma have lower plasma arginine levels, which correlate with inflammation severity. Arginine levels increase during recovery, indicating reduced inflammation.

Area of Science:

  • Biochemistry
  • Pediatric Critical Care
  • Metabolic Disorders

Background:

  • Arginine is a crucial amino acid in metabolic processes, vital for both health and disease states.
  • Reduced arginine levels are frequently observed in children suffering from various critical illnesses.

Purpose of the Study:

  • To investigate the relationship between plasma arginine concentrations and the severity of inflammation in critically ill children.
  • To examine the association between precursor amino acids and inflammation severity in pediatric critical illness.

Main Methods:

  • An observational cohort study was conducted involving critically ill children.
  • Participants included children with viral respiratory disease, accidental or surgical trauma, and sepsis admitted to a pediatric intensive care unit.

Main Results:

  • Plasma arginine and citrulline concentrations were significantly lower in children with sepsis and trauma compared to those with viral disease.
  • Lower arginine and citrulline levels showed a strong inverse correlation with inflammation severity, as indicated by C-reactive protein (CRP) concentrations.
  • During recovery, arginine and citrulline levels increased, correlating with reduced inflammation markers.

Conclusions:

  • Plasma arginine and citrulline levels are diminished during the acute phase of critical illness in children.
  • These amino acid levels normalize during the recovery phase.
  • Plasma arginine and citrulline concentrations are closely linked to the severity of inflammation in critically ill children.
Abstract

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